Found: 159
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Upregulated expression of glucose transporter isoform 1 in invasive and metastatic extramammary Paget's disease.
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- Experimental & Therapeutic Medicine, 2024, v. 27, n. 5, p. N.PAG, doi. 10.3892/etm.2024.12516
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- Article
Pyoderma gangrenosum successfully treated with split‐thickness skin grafting in combination with negative pressure wound therapy: A case report.
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- Journal of Dermatology, 2024, v. 51, n. 5, p. e156, doi. 10.1111/1346-8138.17048
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- Article
Variable clinical consequences of mosaicism for c.1167dupC in IKBKG in male and female patients with incontinentia pigmenti and related phenotypes.
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- Clinical & Experimental Dermatology, 2024, v. 49, n. 3, p. 298, doi. 10.1093/ced/llad358
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- Article
A case of adult‐onset localized recessive dystrophic epidermolysis bullosa, harboring the novel COL7A1 mutation p.G2754E and the previously reported mutation p.R1763.
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- Journal of Dermatology, 2024, v. 51, n. 3, p. e74, doi. 10.1111/1346-8138.16993
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- Article
Acquired cutis laxa secondary to acute generalized exanthematous pustulosis: A case report and mini‐review of literature.
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- Journal of Dermatology, 2024, v. 51, n. 2, p. 287, doi. 10.1111/1346-8138.16860
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- Article
Cost-Effectiveness Analysis of Atezolizumab versus Platinum-Based Chemotherapy as First-Line Treatment for Patients with Unresectable Advanced Non-small Cell Lung Cancer with PD-L1 Expression Status in Japan.
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- Clinical Drug Investigation, 2023, v. 43, n. 11, p. 839, doi. 10.1007/s40261-023-01311-5
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- Article
Involvement of the genus Corynebacterium in the pathogenesis of pigmented intratarsal keratinous cyst.
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- Journal of Dermatology, 2023, v. 50, n. 11, p. 1488, doi. 10.1111/1346-8138.16871
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- Article
Two cases of cutaneous‐type pemphigus vulgaris and a case of pemphigus foliaceus without mucosal involvement despite high anti‐desmoglein 3 autoantibody levels.
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- Journal of Dermatology, 2023, v. 50, n. 11, p. 1501, doi. 10.1111/1346-8138.16907
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- Article
Epidermodysplasia verruciformis with squamous cell carcinomas and the identification of a novel TMC8 mutation.
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- Journal of Dermatology, 2023, v. 50, n. 10, p. e325, doi. 10.1111/1346-8138.16821
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- Article
A severe case of primary erythromelalgia presenting as small fiber neuropathy with a novel SCN9A mutation.
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- Journal of Dermatology, 2023, v. 50, n. 7, p. 938, doi. 10.1111/1346-8138.16754
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- Article
Eruptive melanocytic nevi associated with encorafenib and cetuximab combination therapy.
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- Journal of Dermatology, 2023, v. 50, n. 5, p. e173, doi. 10.1111/1346-8138.16701
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- Article
Author reply to "WNT10A variant and severe scoliosis?".
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- Journal of Dermatology, 2022, v. 49, n. 11, p. e424, doi. 10.1111/1346-8138.16560
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- Article
Recovery From Severe Systemic Peripheral Neuropathy Secondary to Erythropoietic Protoporphyria by Liver Transplant: A Case Report.
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- Experimental & Clinical Transplantation, 2022, v. 20, n. 10, p. 954, doi. 10.6002/ect.2022.0157
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- Article
A mild case of acute generalized exanthematous pustulosis caused by gemcitabine.
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- Journal of Dermatology, 2022, v. 49, n. 8, p. e261, doi. 10.1111/1346-8138.16388
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- Article
Familial Michelin tire baby syndrome.
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- Journal of Dermatology, 2022, v. 49, n. 7, p. e219, doi. 10.1111/1346-8138.16346
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- Article
Three cases of drug‐induced hypersensitivity syndrome associated with mRNA‐based coronavirus disease 2019 vaccines.
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- Journal of Dermatology, 2022, v. 49, n. 6, p. 652, doi. 10.1111/1346-8138.16347
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- Article
Two novel mutations in the ATP2C1 gene found in Japanese patients with Hailey–Hailey disease.
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- Journal of Dermatology, 2022, v. 49, n. 6, p. 656, doi. 10.1111/1346-8138.16353
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- Article
Novel mutation in the UROS gene causing congenital erythropoietic porphyria in an elderly Japanese female.
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- Journal of Dermatology, 2022, v. 49, n. 6, p. e215, doi. 10.1111/1346-8138.16340
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- Article
Novel mutation of the ferrochelatase gene in a Japanese boy with erythropoietic protoporphyria.
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- Journal of Dermatology, 2022, v. 49, n. 5, p. e179, doi. 10.1111/1346-8138.16319
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- Article
Role of phlebotomy in the treatment of liver damage related to erythropoietic porphyria.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-10089-z
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- Article
An epidemiological survey of anhidrotic/hypohidrotic ectodermal dysplasia in Japan: High prevalence of allergic diseases.
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- Journal of Dermatology, 2022, v. 49, n. 4, p. 422, doi. 10.1111/1346-8138.16278
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- Article
Clarithromycin for the treatment of pyoderma gangrenosum associated with myelodysplastic syndrome.
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- Journal of Dermatology, 2022, v. 49, n. 4, p. e131, doi. 10.1111/1346-8138.16267
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- Article
A Case of Darier's Disease with a Novel Missense Mutation in ATP2A2 Successfully Treated with Calcipotriol/Betamethasone Dipropionate Two-Compound Ointment.
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- 2022
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- Publication type:
- Case Study
Availability of mRNA Obtained from Peripheral Blood Mononuclear Cells for Testing Mutation Consequences in Dystrophic Epidermolysis Bullosa.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 24, p. 13369, doi. 10.3390/ijms222413369
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- Article
Two cases of Hailey‐Hailey disease effectively treated with apremilast and a review of reported cases.
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- Journal of Dermatology, 2021, v. 48, n. 12, p. 1945, doi. 10.1111/1346-8138.16178
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- Article
Novel nonsense mutation in the SLC39A4 gene in a Japanese boy with mild acrodermatitis enteropathica.
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- Journal of Dermatology, 2021, v. 48, n. 12, p. e602, doi. 10.1111/1346-8138.16184
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- Article
The second Japanese case of porphyria cutanea tarda with a novel genetic mutation in UROD.
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- Journal of Dermatology, 2021, v. 48, n. 11, p. 1802, doi. 10.1111/1346-8138.16156
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- Article
Case of epidermodysplasia verruciformis with a novel mutation of TMC8.
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- Journal of Dermatology, 2021, v. 48, n. 11, p. e568, doi. 10.1111/1346-8138.16139
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- Article
Atypical eosinophilic annular erythema clinically resembling granuloma annulare.
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- International Journal of Dermatology, 2021, v. 60, n. 10, p. e416, doi. 10.1111/ijd.15591
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- Article
Autoimmune hemolytic anemia during long‐term administration of nivolumab for metastatic melanoma.
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- 2021
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- Case Study
Pembrolizumab-Induced Lichen Planus on the Scalp of a Patient with Non-Small-Cell Lung Carcinoma.
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- 2021
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- Publication type:
- Case Study
Widespread kerosene dermatitis associated with rhabdomyolysis.
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- Journal of Dermatology, 2021, v. 48, n. 8, p. e386, doi. 10.1111/1346-8138.15956
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- Article
Management of keratoacanthoma with perineural invasion: case reports and literature review.
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- Australasian Journal of Dermatology, 2021, v. 62, n. 2, p. e353, doi. 10.1111/ajd.13550
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- Article
Significance of IL36RN mutation analyses in the management of impetigo herpetiformis: A case report and review of published cases.
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- Journal of Dermatology, 2021, v. 48, n. 5, p. 699, doi. 10.1111/1346-8138.15788
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- Article
Novel gross deletion mutation c.‐105_4042+498del in the TNXB gene in a Japanese woman with classical‐like Ehlers–Danlos syndrome: A case of uneventful pregnancy and delivery.
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- Journal of Dermatology, 2021, v. 48, n. 5, p. e227, doi. 10.1111/1346-8138.15837
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- Article
Pseudosyndactyly and digital contractures in bullous pemphigoid with anti‐BP180‐C‐terminal domain autoantibodies.
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- Journal of Dermatology, 2021, v. 48, n. 5, p. e229, doi. 10.1111/1346-8138.15842
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- Article
Novel ATP2A2 nonsense mutation in a Japanese case with Darier's disease.
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- Journal of Dermatology, 2021, v. 48, n. 3, p. e149, doi. 10.1111/1346-8138.15760
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- Article
Novel ATP2C1 frame‐shift mutation in a mild case of early onset sporadic Hailey–Hailey disease.
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- Journal of Dermatology, 2021, v. 48, n. 2, p. e96, doi. 10.1111/1346-8138.15689
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- Article
Clinical practice guide for the treatment of perforating dermatosis.
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- Journal of Dermatology, 2020, v. 47, n. 12, p. 1374, doi. 10.1111/1346-8138.15647
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- Article
Crouzon syndrome with acanthosis nigricans and prominent diffuse hyperpigmentation associated with gain‐of‐function A391E mutation in FGFR3 gene.
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- Journal of Dermatology, 2020, v. 47, n. 12, p. e451, doi. 10.1111/1346-8138.15580
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- Article
Novel TGM1 Gene Mutation in a Japanese Patient with Bathing Suit Ichthyosis.
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- 2020
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- Case Study
Benign neonatal hemangiomatosis with early regression of skin lesions: A case report and review of the published work.
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- Journal of Dermatology, 2020, v. 47, n. 8, p. 911, doi. 10.1111/1346-8138.15413
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- Article
Japanese case of Papillon–Lefèvre syndrome with novel compound heterozygous mutations.
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- Journal of Dermatology, 2020, v. 47, n. 8, p. e293, doi. 10.1111/1346-8138.15412
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- Article
Partial spontaneous regression of pediatric large fibroblastic connective tissue nevus.
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- Journal of Dermatology, 2020, v. 47, n. 6, p. e232, doi. 10.1111/1346-8138.15320
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- Article
Abnormal keratinization and cutaneous inflammation in Mal de Meleda.
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- Journal of Dermatology, 2020, v. 47, n. 5, p. 554, doi. 10.1111/1346-8138.15296
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- Article
Novel mutation of the ferrochelatase gene in a Japanese family with erythropoietic protoporphyria.
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- Journal of Dermatology, 2020, v. 47, n. 4, p. e114, doi. 10.1111/1346-8138.15258
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- Article
Case of bullous pemphigoid following Hailey–Hailey disease with novel mutation of the ATP2C1 gene.
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- Journal of Dermatology, 2020, v. 47, n. 3, p. e79, doi. 10.1111/1346-8138.15229
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- Article
Pedunculated aneurysmal fibrous histiocytoma with increased <sup>18</sup>F‐fluorodeoxyglucose uptake on positron emission tomography/computed tomography.
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- Journal of Dermatology, 2020, v. 47, n. 3, p. e100, doi. 10.1111/1346-8138.15237
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- Article
Paraneoplastic syndrome associated with chronic myelogenous leukemia mimicking adult‐onset Still's disease.
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- Journal of Dermatology, 2020, v. 47, n. 2, p. e67, doi. 10.1111/1346-8138.15169
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- Article
Case of Hailey‐Hailey disease with a novel missense/in‐frame deletion mutation in ATP2C1 successfully treated with cyclosporine.
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- Journal of Dermatology, 2019, v. 46, n. 12, p. e482, doi. 10.1111/1346-8138.15081
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- Article